Epilepsy
Study register · detail Kohortenstudie · Epilepsy · 2025

UK Medical Cannabis Registry: A Clinical Outcomes Analysis for Epilepsy.

Clear benefit GRADE Low 1 citations
Samplen = 134 Pat.
Duration6 months
EndpointQOLIE-31
Blindingn.a.
DesignKohortenstudie
Key finding

Cannabis-based medicinal products were associated with improvements in all measured quality of life and health parameters (QOILE-31, sleep quality, EQ-5D-5L, anxiety, global impression); 29,85% of patients achieved clinically meaningful improvement.

Summary

UK Medical Cannabis Registry: Case series (n=134) on cannabis-based medicinal products (CBMPs) in treatment-resistant epilepsy. Improvements in QOLIE-31 and all HRQoL PROMs (p<0,050) at 1, 3 and 6 months vs. baseline; 40 patients (29,85%) achieved a clinically relevant difference in QOLIE-31 after 6 months. 18 adverse events (13,43%) in 5 patients (3,73%), predominantly mild/moderate.

P
PopulationAdults with treatment-resistant epilepsy from the UK Medical Cannabis Registry, n=134
I
InterventionCannabis-based medicinal products (CBMPs), type/dose not further specified
O
OutcomeSignificant improvements in QOLIE-31 and all HRQoL PROMs from baseline to 1, 3 and 6 months (p<0,050); 29,85% of patients achieved a clinically relevant difference in QOLIE-31 after 6 months; 18 AEs in 5 patients (3,73%), predominantly mild to moderate
Confidence in the evidence
Low

The second of four GRADE levels, the effect estimate is of limited reliability.

Quality profile
Sample size
Blinding
Effect size Clear benefit
Citations / year
Authors
Cowley I, Erridge S, Aggarwal A, Evans L, Varadpande M, Clarke E, McLachlan K, Coomber R, Iqbal A, Rucker JJ
DOI 10.1002/brb3.70490
Design: Kohortenstudie
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Abstract
Background: A third of epilepsy patients fail to enter seizure remission despite optimal therapeutic management. Cannabis-based medicinal products (CBMPs) have shown promise as a potential therapy. However, a paucity of high-quality literature regarding CBMPs' efficacy and safety profile means further investigation is needed. The study aimed to examine changes in epilepsy-specific and general health-related quality of life (HRQoL) patient-reported outcome measures (PROMs) in individuals with treatment-resistant epilepsy. Methods: A case series of patients with epilepsy from the UK Medical Cannabis Registry analyzed changes in Quality of Life in Epilpesy-31 (QOILE-31), Single-Item Sleep Quality Score (SQS), EQ-5D-5L, Generalized Anxiety Disorder-7 (GAD-7) and Patient Global Impression of Change (PGIC) between baseline, one, three, and six months. Adverse events (AEs) were collected and classified by severity. p < 0.050 was considered statistically significant. Results: There were 134 patients included. Improvements were recorded from baseline to one, three, and six months in QOILE-31 and all HRQoL PROMs (p < 0.050). Forty patients (29.85%) reported a minimal clinically important difference in Quality of Life in Epilepsy-31 (QOLIE-31) at six months. There were 18 (13.43%) AEs reported by 5 (3.73%) patients, mainly mild and moderate. Discussion: The proportion of patients achieving a clinically significant change is similar to existing CBMPs in epilepsy literature. AE incidence was lower than similar studies although this may be due to the large proportion (67.16%) of individuals who were not cannabis naive. Conclusion: Initiation of CBMPs was associated with an improvement across all PROMs. CBMPs were well tolerated across the cohort. However, randomized controlled trials are needed to help determine causality.

The impediment to action advances action. — Marcus Aurelius